JPS5915884B2 - herbicide - Google Patents
herbicideInfo
- Publication number
- JPS5915884B2 JPS5915884B2 JP56010282A JP1028281A JPS5915884B2 JP S5915884 B2 JPS5915884 B2 JP S5915884B2 JP 56010282 A JP56010282 A JP 56010282A JP 1028281 A JP1028281 A JP 1028281A JP S5915884 B2 JPS5915884 B2 JP S5915884B2
- Authority
- JP
- Japan
- Prior art keywords
- plants
- herbicide
- effect
- damage
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- A01N35/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N45/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
- A01N45/02—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring having three carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【発明の詳細な説明】
本発明は有効物質よりなる混合物を含有する除草剤に係
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a herbicide containing a mixture of active substances.
置換された安息香酸及びベンツチオチアジアジノンが除
草作用を有することは公知である。It is known that substituted benzoic acids and benzothiothiadiazinones have herbicidal activity.
しかしその除草作用は後述の実施例に示すように好まし
いものではない。However, its herbicidal action is not desirable as shown in the Examples below.
しかるに −
(a)
(式中Rは炭素原子4個までを有する低級アルキル残基
を意味する)の化合物又はその塩例えばアルカリ−、ア
ルカリ土類−、アンモニウム−、ヒドロキシアルキル−
又はアルキルアンモニウム−及びヒドラジン塩、例えば
ナトリウム、リチウム、カリウム、カルシウム、鉄、メ
チルアンモニウム、トリメチルアンモニウム、エチルア
ンモニウム、ジェタノールアンモニウム、エタノールア
ンモニウム、ジメチルアミン、ジメチルエタノールアミ
ン、ヒドラジン又はフェニルヒドラジンとの塩及び
(b)式
(式中Xはハロゲン、メトキシ又はアミノを意味し、n
は1.2.3又は4を意味し、この場合メトキシ及びハ
ロゲン又はアミノ及びハロゲン又はメトキシ、アミノ及
びハロゲンは同時に存在することができる)の化合物
よりなる混合物は個々の有効物質よりも良好な除草作用
を有することが知られた。However, - (a) compounds of the formula (wherein R means a lower alkyl residue having up to 4 carbon atoms) or salts thereof, such as alkali-, alkaline-earth-, ammonium-, hydroxyalkyl-
or alkylammonium and hydrazine salts, such as sodium, lithium, potassium, calcium, iron, methylammonium, trimethylammonium, ethylammonium, jetanolammonium, ethanolammonium, dimethylamine, dimethylethanolamine, hydrazine or phenylhydrazine; (b) Formula (wherein X means halogen, methoxy or amino, n
means 1.2.3 or 4, in which case mixtures of the compounds methoxy and halogen or amino and halogen or methoxy, amino and halogen can be present simultaneously) are better herbicidal than the individual active substances. It is known to have an effect.
有効物質a及びbは1ヘクタールにつき0.5乃至5ゆ
の量に於て使用されることができる。Active substances a and b can be used in amounts of 0.5 to 5 yu per hectare.
有効物質の混合比は5:1乃至1:5、殊に3:1乃至
1:3重量部である。The mixing ratio of the active substances is 5:1 to 1:5, in particular 3:1 to 1:3 parts by weight.
゛混合物は有用植物例えば穀物、稲、大豆、玉蜀黍
、馬鈴薯、エン豆及びソラ豆の栽培に於て望ましからぬ
植物例えば双子葉雑草、単子葉非草本類又はハマスゲ類
の駆除に適する。The mixture is suitable for the control of undesirable plants such as dicotyledonous weeds, monocotyledonous non-herbaceous plants or sedges in the cultivation of useful plants such as cereals, rice, soybeans, onions, potatoes, peas and faba beans.
混合物は前発芽法に於て及び(又は)係発芽法忙於て使
用されることができる。The mixture can be used in a pre-germination method and/or in a sub-germination method.
有効物質は溶液、乳濁液、懸濁液、油分散液、噴霧剤又
は粒状体として使用されることができる。The active substances can be used as solutions, emulsions, suspensions, oil dispersions, sprays or granules.
使用形は完全に使用目的に適合せしめられる。The form of use is completely adapted to the intended use.
使用形は如何なる場合にも有効物質の細分布を保証しな
ければならない。The form of use must in all cases ensure a fine distribution of the active substance.
直接散布し得る溶液を製造するためには、中位又は高位
の沸点を有する鉱油溜分例えば溶油又はディーゼル油、
更にコールタール油並びに植物性又は動物性産出源の油
、更に環状炭化水素例えばテトラヒドロナフタリン及び
アルキル置換ナフタリンが使用される。In order to produce directly sprayable solutions, mineral oil fractions with medium or high boiling points, such as melt oil or diesel oil, can be used.
Also used are coal tar oil and oils of vegetable or animal origin, as well as cyclic hydrocarbons such as tetrahydronaphthalene and alkyl-substituted naphthalene.
水性使用形は、乳濁液濃縮物、ペースト又は湿潤可能の
粉末(噴射粉末)より水の添加により製造されることが
できる。Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (spray powders) by addition of water.
乳濁液を製造するためには、物質をそのまま又は溶剤中
に溶解して、湿潤剤又は分散剤により水中に均質に混合
することができる。To produce emulsions, the substances can be mixed homogeneously in water with the aid of wetting or dispersing agents, either neat or dissolved in a solvent.
しかも有効物質、湿潤剤、附着剤、乳化剤又は分散剤及
び場合により溶剤よりなる濃縮物も製造されることがで
き、これは水にて稀釈するのに適する。In addition, concentrates of active substance, wetting agents, adhesion agents, emulsifiers or dispersants and, if appropriate, solvents, can also be prepared, which are suitable for dilution with water.
できあがった噴射液に種々のタイプの油を添加すること
ができる。Various types of oil can be added to the finished propellant.
噴霧剤は、有効物質と固状担体物質例えば粘土又は肥料
とを混合又は一緒に磨砕することにより製造されること
ができる。Sprays can be produced by mixing or grinding together the active substance and a solid carrier material, such as clay or fertilizer.
粒状体は有効物質を固状担体物質に結合することにより
製造されることができる。Granules can be produced by binding the active substance to a solid carrier material.
更に油を使用して直接散布し得る分散液を製造すること
ができる。Furthermore, oils can be used to prepare dispersions that can be directly sprayed.
有効物質は肥料、殺虫剤、殺菌剤又は他の除草剤と混合
されることができる。The active substances can be mixed with fertilizers, pesticides, fungicides or other herbicides.
本発明混合剤の除草効果について実施例を示し、単剤と
の比較において説明する。Examples of the herbicidal effect of the mixture of the present invention will be explained in comparison with a single agent.
実施例 1
植物、稲(0ryza 5ativa ) 、大豆(
5ojahispida )、玉蜀黍(Zea may
s ) 、、小麦(Triticum aestivu
m )、キビ(Echinochloacrus g
alli)、、アキノエノコログサ(Setariaf
aberii )、食用)S−qスゲ(Cyperus
eseulentus ) 、ペンシルバニア・オナモ
ミ(Xanthium pensylvanicum
) 、ノガラシ(5inapis arvensis
)%サジオモガタ(Alisma plantag
o −aquatica ) 、ヤエムグラ(Gali
um aparine ) 、カミルレ(Matrie
ariacharnomilla )、センニンニク(
A lopecurusmyosuroides )及
び1年少スズメノカタビラ(Poa annus )
を4乃至20crILの生長高さに於て次の個々の有効
物質及びその混合物にて夫々1ヘクタールにつき水50
0J中に乳濁又は分散して処理した:
I 2・3・6−ドリクロルー安息香酸、1ヘクタール
につき有効物質0.5及び2kg
■ 2−メトキシ−3・6−ジクロル−安息香酸、1ヘ
クタールにつき有効物質1.5及び2kgIII 3
−イソプロピル−2・1・3−ペン/”−チアジアジノ
ン−(4)−2・2−ジオキシド、1ヘクタールにつき
有効物質0.5.1.1.5、r 2及び3kg
I+ll11ヘクタールにつき有効物質0.5 +1.
5g
n十m 1ヘクタールにつき有効物質1.5+0.5
g
次の第1表より混合物は8乃至14日後個々の有効物質
に比し有利な栽培植物忍容性に於て良好な同作用を示す
ことを認めることができる。Example 1 Plants, rice (0ryza 5ativa), soybean (
5ojahispida), Zea may
s),, wheat (Triticum aestivu)
m), millet (Echinochloacrus g
alli), Setariaf
aberii), edible) S-q sedge (Cyperus
Xantium pensylvanicum
), 5inapis arvensis
)%Alisma plantag
o -aquatica), Yaemugura (Gali
um aparine), Camille (Matrie)
ariacharnomilla), Sengarlic (
A lopecurus myosuroides) and one-year-old sparrowfly (Poa annus)
at a growth height of 4 to 20 crIL with the following individual active substances and mixtures thereof, each with 50 liters of water per hectare.
Treated as emulsion or dispersion in 0J: I 2,3,6-dichlorobenzoic acid, 0.5 and 2 kg of active substance per hectare ■ 2-methoxy-3,6-dichlorobenzoic acid, per hectare Active substance 1.5 and 2 kg III 3
-isopropyl-2,1,3-pen/”-thiadiazinone-(4)-2,2-dioxide, 0.5.1.1.5 active substance per hectare, r 2 and 3 kg I+ll 0 active substance per 11 ha .5 +1.
5g n10m 1.5 + 0.5 active substance per hectare
g It can be seen from the following Table 1 that the mixture exhibits a better effect on cultivated plant tolerance than the individual active substances after 8 to 14 days.
第1表の試験成績について
除草剤は一般に対象植物を完全又は完全に近く損傷する
のでなければ意味がない、何んとなれば完全に損傷され
ず生き残れば、後日回復し大きくなって害を及ぼし除草
剤としての効果は半減する。Regarding the test results in Table 1, herbicides are generally meaningless unless they completely or nearly completely damage the target plants.If they survive without being completely damaged, they will recover later and grow larger and cause more damage. Its effectiveness as a herbicide is halved.
又一方で一剤でできるだけ多くの種類の雑草な枯殺でき
る殺草スペクトルの巾の広い除草剤の要望がある。On the other hand, there is a need for a herbicide with a broad spectrum of weeds that can kill as many types of weeds as possible with a single agent.
即ち除草剤は対象植物を完全に枯殺し、しかも有用植物
には全(害を与えず、更に対象有害植物の巾換言すれば
殺草スペクトルの巾が広いことが望まれている。In other words, it is desired that herbicides completely kill target plants, do no harm to useful plants, and have a broad herbicidal spectrum that covers the target harmful plants.
以上の観点から、この試験成績即ち効果を観察する。From the above viewpoints, we will observe the test results, that is, the effects.
除草剤1は単独で使用した場合、2 kg/ ha使用
しないと望ましくない植物に対して完全又は完全に近い
損傷割合を示さないが、この使用量では有用植物、例え
ば小麦に対して害(2o)を与える。Herbicide 1, when used alone, does not show complete or near-complete damage to undesirable plants unless applied at 2 kg/ha, but at this amount it does not cause harm (20 kg/ha) to useful plants, such as wheat. )give.
したがって2kg/ha使用することには問題がある。Therefore, there is a problem in using 2 kg/ha.
又同様にして除草剤■も2 kg/ ha使用しないと
所望の効果は得られないが、上記と同様に有用植物小麦
に対して有害(15)であり問題である。Similarly, the desired effect cannot be obtained with the herbicide ① unless it is used at 2 kg/ha, but it is also harmful to the useful plant wheat (15), which is a problem.
即ち両薬剤は共に2 kg/ ha以下しか使用できず
、一方それ以下の使用では所望の効果が得られないとい
う欠点がある。That is, both drugs can only be used in amounts of 2 kg/ha or less, and on the other hand, they have the disadvantage that the desired effects cannot be obtained when used in amounts less than 2 kg/ha.
ところで除草剤■は3 kg/ha使用しないと所望の
効果は得られないが、これだけ使用しても、センニンニ
ク及びスズメノカタビラに対しては、殆んど除草効果を
示さない。By the way, the desired effect cannot be obtained with the herbicide (3) unless it is used at a rate of 3 kg/ha, but even if this amount is used, it shows almost no herbicidal effect on Garlic and Psyllium.
ところが除草剤■又は■を除草剤■との混合剤として使
用した場合は、例えば■を0.5kg/ha 、 mを
1.5に9/ha 、或いは■を1.5kg/ ha
、 y1ヲ0、5 kg/ ha という少量宛の
使用で、有用植物に対して害がなく、好ましくない植物
を完全又は完全に近(損傷することができる。However, when herbicide ■ or ■ is used as a mixture with herbicide ■, for example, ■ is 0.5 kg/ha, m is 1.5 to 9/ha, or ■ is 1.5 kg/ha.
When used in small amounts of 0.5 kg/ha, it is harmless to useful plants and can completely or nearly completely damage undesirable plants.
即ち本発明薬剤は、個々の薬剤により所望効果が得られ
る量よりモ極めて少量で、かつ巾広い範囲で好ましくな
い植物を完全もしくは完全に近く損傷することができ、
しかも有用植物に対し薬害を与えないものである。In other words, the chemicals of the present invention can completely or nearly completely damage undesirable plants over a wide range and in a much smaller amount than the amount required to achieve the desired effect with each individual chemical.
Moreover, it does not cause any phytotoxicity to useful plants.
このような相剰作用の発現の根拠は、それが浸透性の増
大に基づくものか、最終的の第三次成分の生成によるも
のであるのか明らかでないが、極めて顕著な相剰作用の
発生の結果によるものであることは明らかである。The basis for the occurrence of such a mutual effect is not clear whether it is based on increased permeability or the final formation of a tertiary component, but it is clear that the basis for the occurrence of such a mutual effect is extremely significant. It is clear that this is due to the results.
実施例 2
露地において発芽後栽培植物、大豆(5ojahisp
ida )及び玉蜀黍(Zea mays )及び望ま
しからぬ植物、キビ(Echinochloa cr
us galli)、アキノエノ=roグサ(5et
aria faberii )、食用ハマスゲ(Cy
perus esculentus ) 、ノガラシ
(5inapis arvensis )、ペンシル
バニア・オナモミ(Xanthium pensylv
anicum ) 、ヤエムグラ(Galium ap
arine )、カミルレ(Matricariach
amomilla )、ドイツ生ホソムギ(Loliu
mperenne )及び大スズメノカタビラ(Poa
trivialis )を次の個々の有効物質及びその
混合物にて処理した:
13−イソプロピル−2・1・3−ベンゾ−チアジアジ
ノン−(4)−2・2−ジオキシド、1ヘクタールにつ
き有効物質0.7及び2kg■ 3−アミノ−2・5−
ジクロル−安息香酸、1ヘクタールにつき有効物質1.
3及び2kg1+■ 1ヘクタールにつき有効物質0.
7 +1.3g
10乃至14日後、混合物I+I[は個々の有効物質■
及び■よりも栽培植物に於て良好な愚答性を示し、且つ
良好な除草作用を示したことが確認された。Example 2 Plants cultivated after germination in open field, soybean (5 ojahisp
ida) and Zea mays and undesirable plants, Millet (Echinochloa cr
us galli), Akinoeno=rogusa (5et
aria faberii), edible sedge (Cy
perus esculentus), Xantium pensylv (5inapis arvensis),
anicum), Yaemugura (Galium ap)
arine), Camille (Matricariach)
amomilla), German raw barley (Loliu
mperenne) and Great Sparrow (Poa
trivialis) was treated with the following individual active substances and mixtures thereof: 13-isopropyl-2,1,3-benzo-thiadiazinone-(4)-2,2-dioxide, 0.7 active substance per hectare and 2kg ■ 3-Amino-2・5-
Dichlorobenzoic acid, 1. active substance per hectare.
3 and 2 kg 1+■ 0.0 active substance per hectare.
7 + 1.3 g After 10-14 days, mixture I + I [is the individual active substance ■
It was confirmed that it showed better reactivity in cultivated plants and better herbicidal action than those of (1) and (2).
試験結果は次の第2表より認められることができる。The test results can be seen from Table 2 below.
第2表の試験成績について
実施例1の第1表について述べたと同様に極めて顕著な
相剰作用を示すことが認められる。Regarding the test results in Table 2, it is recognized that, as described in Table 1 of Example 1, a very significant synergistic effect is exhibited.
薬剤Iは2 kg/ ha使用してはじめて食用ハマス
ゲ、ノガラシ、ペンシルバニア・オナモミ、ヤエムグラ
、カミルレに対し75.80.90.80.80の損傷
割合を示すが、ドイツ生ホソムギ、大スズメノカタビラ
に対しては損傷割合はOである。Drug I showed a damage rate of 75.80.90.80.80 for edible Japanese porphyry, Japanese turmeric, Pennsylvanian mullet, and Camille only after 2 kg/ha was used, but it had a damage rate of 75.80.90.80.80 for German raw barley and Psyllium japonica. The damage rate is O.
一方薬剤■は2kg/ha使用することによりアキノエ
ノコログサ、ドイツ生ホソムギ、大スズメノカタビラに
対し80.70.80の損傷割合を示すが食用ハマスゲ
、ノガラシ、ペンシルバニア・オナモミ、ヤエムグラ、
カミルレに対して10.30.10.10.10の損傷
割合しか示さない。On the other hand, when the drug ■ is used at 2 kg/ha, it shows a damage rate of 80.70.80 against Aquinofolia, German native wheat, and Psyllium japonica, but it also shows a damage rate of 80.70.80 on edible Japanese commonweed, Nogarashi, Pennsylvanian firium, and Yaemugura.
It only shows a damage ratio of 10.30.10.10.10 for Camille.
したがって、相剰効来がないとすれば相加的に考えた場
合Iを2 kg/ha Jを2 kg/ha即ち合計4
kl?/ ha使用することにより100又は100
に近い効果を示すはずであるが、表に示す如くIを0.
7kg/ha 、 [Iを1.3kg/ha計2kg/
ha即ち、必要使用量と目される4 kg/ ha の
半分の量即ち極端に少ない量を使用することによりアキ
ノエノコログサ、食用ハマスゲ、ノガラシ、ペンシルバ
ニア・オナモミ、ヤエムグラ、カミルレ、ドイツ生ホソ
ムギ、大スズメノカタビラのそれぞれに対し90.90
.100.100.85.95.70.90の損傷割合
即ち完全又は完全に近い損傷割合を示し、しかも有用植
物である大豆、玉蜀黍に対しては全く害を及ぼしていな
い。Therefore, assuming that there is no mutual effect, considering it additively, I is 2 kg/ha, J is 2 kg/ha, or a total of 4
kl? 100 or 100 by using / ha
However, as shown in the table, if I is set to 0.
7kg/ha, [I 1.3kg/ha total 2kg/ha]
ha, that is, half of the required usage amount of 4 kg/ha, that is, an extremely small amount, can be used to reduce the amount of red foxtail, edible red mullet, cypress, Pennsylvania staghorn, Japanese snail, Camille, German raw barley, and large sycamore. 90.90 for each
.. It shows a damage ratio of 100.100.85.95.70.90, that is, a complete or nearly complete damage ratio, and does not cause any harm to useful plants such as soybean and corn.
以上のようにこの例においても本発明除草剤が顕著な相
剰効果を示すことがわかる。As described above, it can be seen that the herbicide of the present invention exhibits a remarkable synergistic effect in this example as well.
実施例 3
温室で大麦(Hordeum ) 、ライ麦(5eca
le )、小麦(Triticum aestivum
)および、望ましくない植物であるヤエムグラ(Ga
lium aparine )およびセンニン0り(A
lopecurus myosuroides )の発
芽後、これらの植物と地面を下記の単一物質とその混合
物で処理する。Example 3 Barley (Hordeum), rye (5 eca
le ), wheat (Triticum aestivum
) and the undesirable plant Ga
lium aparine) and sennin 0li (A
After germination of L. lopecurus myosuroides, these plants and the ground are treated with the following single substances and mixtures thereof.
A 3−fソプロピル−2・1・3−ベンゾチアジア
ジノン−(4) −2・2−ジオキシド活性物質0.5
.0.75、■、0、i、 5 kg/ haB 2・
5−ジクロール−6−メトキシ安息香酸(ジメチルアン
モニウム塩)活性物質0.5.0.75.1.0.1.
5kg/ha
〜A+B 0.5+1.0.1.0+0.5.0.7
5+0、75 kg/ ha
10〜14日後に混合物は栽培植物に対して同一の条件
下で除草作用が顕著に優れていることが確認された。A 3-f sopropyl-2,1,3-benzothiadiazinone-(4) -2,2-dioxide active substance 0.5
.. 0.75, ■, 0, i, 5 kg/haB 2.
5-Dichloro-6-methoxybenzoic acid (dimethylammonium salt) active substance 0.5.0.75.1.0.1.
5kg/ha ~A+B 0.5+1.0.1.0+0.5.0.7
5+0, 75 kg/ha After 10-14 days, it was confirmed that the mixture had significantly better herbicidal activity on cultivated plants under the same conditions.
試験結果を次の第3表に示す。第3表の試験成績につい
て
Aを1.5 kg/ ha使用してもヤエムグラ、セン
ニンニクに対して60.10の損傷割合、又Bを1、5
kg/ ha 使用しても同植物に対して60.4
5の効果しか示さない。The test results are shown in Table 3 below. Regarding the test results in Table 3, even if A was used at 1.5 kg/ha, the damage rate was 60.10 for Yaemugura and Sengaric, and B was 1.5 kg/ha.
kg/ha for the same plant even if used
Shows only 5 effects.
即ち実施例1において述べたように除草効果即ち損傷効
果は100又はそれに近い数値が望まれるものであるか
ら、より高い即ち100又はそれに近い損傷効果を得よ
うとすれば、この量の使用では相当量に不足であること
が明らかである。That is, as mentioned in Example 1, the herbicidal effect, that is, the damage effect, is desired to be a value of 100 or close to it, so if you want to obtain a higher damage effect, that is, a damage effect of 100 or close to it, using this amount is quite difficult. It is clear that the quantity is insufficient.
この場合センニンニクに対して損傷効果の高いBを増量
することは、有用植物に対して、より薬害が高まること
は当然に予測され、1.5kg/ha より以上の使
用は避けるべきである。In this case, it is naturally predicted that increasing the amount of B, which has a high damaging effect on garlic, will cause more damage to useful plants, and use of more than 1.5 kg/ha should be avoided.
ところで第3表の下方欄に示すようにA、B剤を混合剤
として使用した場合には、それぞれな単剤で使用した場
合、到底除草剤として望ましい効果を示さない量、即ち
合計量で1.5 kg/ haを使用してもヤエムグラ
、センニンニクに対して100.80の損傷割合を示し
、しかも有用植物は全(損傷しない。By the way, as shown in the lower column of Table 3, when Agents A and B are used as a mixture, when each agent is used alone, it does not show the desired effect as a herbicide, that is, the total amount is 1. Even if 0.5 kg/ha was used, the damage rate was 100.80 for Jaeger and Garlic, and all useful plants were not damaged.
そしてその配合比A:Bが1:2.1:1.2:1のい
ずれであっても望ましくない植物に対して殆んど同様の
効果を示している。And, regardless of whether the blending ratio A:B is 1:2.1:1.2:1, almost the same effect on undesirable plants is shown.
このことは両側を混合することにより顕著な相剰効果は
勿論、その効果には質的変化があることを示すものであ
る。This shows that by mixing both sides, there is not only a significant mutual effect but also a qualitative change in the effect.
以上のように、本発明に係るベンツチオチアジノンと置
換された安息香酸との混合剤は、互いに除草効力を強め
合い顕著な相剰効果を示し、それぞれ単剤における使用
薬量を顕著に節減することができるので農業上きわめて
有用な発明である。As described above, the mixture of benzothiothiazinone and substituted benzoic acid according to the present invention mutually enhances herbicidal efficacy, exhibits a remarkable synergistic effect, and significantly reduces the amount of each drug used as a single agent. This invention is extremely useful in agriculture.
Claims (1)
を意味する。 )の化合物又はその塩及び (b)式 (式中Xはハロゲン、メトキシ又はアミノを意味し、n
は1.2.3又は4を意味し、この場合メトキシ及びハ
ロゲン又はアミノ及びハロゲン又はメトキシ、アミノ及
びハロゲンは同時に存在することができる。 )の化合物よりなる混合物を含有すること−を特徴とす
る除草剤。 23−イングロビル−2・1・3−ベンゾチアジノン−
(4)−2・2ジオキシドと3・6−ジクロル−2−メ
トキシ安息香酸、またはこの酸の塩からなる混合物を含
有することを特徴とする特許請求範囲第1項に記載の除
草剤。 3 3−イングロビル−2・1・3−ベンゾチアジアジ
ノン−(4−)−2・2−ジオキシドと3・6−ジクロ
ル−2−メトキシ安息香酸またはこの酸の塩の重量比が
1:3〜3:1部であることを特徴とする特許請求の範
囲第2iに記載の除草剤。[Claims] 1. Compounds of formula (a) (wherein R means a lower alkyl residue having up to 4 carbon atoms) or a salt thereof and formula (b) (wherein X is halogen, methoxy or amino, n
means 1.2.3 or 4, in which case methoxy and halogen or amino and halogen or methoxy, amino and halogen can be present simultaneously. ) A herbicide characterized by containing a mixture of the following compounds. 23-Inglovir-2,1,3-benzothiazinone-
(4) The herbicide according to claim 1, which contains a mixture of -2,2 dioxide and 3,6-dichloro-2-methoxybenzoic acid, or a salt of this acid. 3 The weight ratio of 3-Inglovir-2,1,3-benzothiadiazinone-(4-)-2,2-dioxide and 3,6-dichloro-2-methoxybenzoic acid or a salt of this acid is 1:3 -3:1 part herbicide according to claim 2i.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE22177226 | 1972-04-13 | ||
| DE2217722A DE2217722C2 (en) | 1972-04-13 | 1972-04-13 | herbicide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56131502A JPS56131502A (en) | 1981-10-15 |
| JPS5915884B2 true JPS5915884B2 (en) | 1984-04-12 |
Family
ID=5841784
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP48031078A Pending JPS4914636A (en) | 1972-04-13 | 1973-03-19 | |
| JP56010282A Expired JPS5915884B2 (en) | 1972-04-13 | 1981-01-28 | herbicide |
| JP1028381A Pending JPS56131503A (en) | 1972-04-13 | 1981-01-28 | Herbicide |
| JP1028481A Pending JPS56131504A (en) | 1972-04-13 | 1981-01-28 | Herbicide |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP48031078A Pending JPS4914636A (en) | 1972-04-13 | 1973-03-19 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1028381A Pending JPS56131503A (en) | 1972-04-13 | 1981-01-28 | Herbicide |
| JP1028481A Pending JPS56131504A (en) | 1972-04-13 | 1981-01-28 | Herbicide |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US3888655A (en) |
| JP (4) | JPS4914636A (en) |
| AR (1) | AR213606A1 (en) |
| AT (7) | AT327606B (en) |
| BE (1) | BE798204A (en) |
| BG (8) | BG20752A3 (en) |
| BR (1) | BR7302710D0 (en) |
| CA (1) | CA1018789A (en) |
| CH (1) | CH575707A5 (en) |
| CS (1) | CS192461B2 (en) |
| DE (1) | DE2217722C2 (en) |
| DK (1) | DK137702C (en) |
| EG (1) | EG11078A (en) |
| ES (1) | ES413606A1 (en) |
| FR (1) | FR2180097B1 (en) |
| GB (1) | GB1417279A (en) |
| HU (1) | HU166808B (en) |
| IL (1) | IL41840A (en) |
| IT (1) | IT980159B (en) |
| KE (1) | KE2630A (en) |
| MY (1) | MY7600183A (en) |
| NL (1) | NL182772C (en) |
| OA (1) | OA04402A (en) |
| PH (1) | PH10948A (en) |
| PL (7) | PL91868B1 (en) |
| SE (3) | SE388754B (en) |
| SU (8) | SU522767A3 (en) |
| TR (1) | TR17279A (en) |
| ZA (1) | ZA732518B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6136793U (en) * | 1984-08-10 | 1986-03-07 | 日吉工業株式会社 | Connection structure of high pressure hose and fittings |
| JPS6252390U (en) * | 1985-09-20 | 1987-04-01 | ||
| JPH0464687U (en) * | 1990-10-17 | 1992-06-03 |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54126686A (en) * | 1978-03-24 | 1979-10-02 | Matsuyama Sekyu Kagaku Kk | Method of recovering liquid phase oxidating catalyst |
| DE4315878A1 (en) * | 1993-05-12 | 1994-11-17 | Basf Ag | Magnesium salt of 3-isopropyl-2,1,3-benzothiadiazin-4-one-2,2-dioxide, process for its preparation and its use for controlling unwanted vegetation |
| EP0714839B1 (en) * | 1994-11-28 | 1998-08-05 | Elpatronic Ag | Process for putting a can welding machine into operation or for converting the same, and a modular magazine for implementing the process |
| DE19505036A1 (en) * | 1995-02-15 | 1996-08-22 | Basf Ag | Process for the preparation of ammonium salts of 3-isopropyl-2,1,3-benzothidadizin-4-one-2,2-dioxide |
| US6218337B1 (en) | 1996-09-27 | 2001-04-17 | Basf Aktiengesellschaft | Solid mixtures of 3-isopropyl-2,1,3-benzothiadiazin-4-one-2,2,-dioxide or its salts |
| WO2004060067A1 (en) * | 2002-12-16 | 2004-07-22 | Valent Biosciences Corporation | Herbicidal composition comprising a ps-ii inhibitor and sar inducer |
| JP5291879B2 (en) * | 2003-03-13 | 2013-09-18 | ビーエーエスエフ ソシエタス・ヨーロピア | Herbicide mixture |
| CN104478829A (en) * | 2014-11-12 | 2015-04-01 | 浙江中山化工集团股份有限公司 | Preparation method of bentazone dimethylamine salt raw drug |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE572662A (en) * | 1957-11-05 | |||
| US3708277A (en) * | 1966-08-30 | 1973-01-02 | Basf Ag | Herbicidal method |
| DE1913266C2 (en) * | 1969-03-15 | 1985-07-18 | Basf Ag, 6700 Ludwigshafen | herbicide |
| DE1913850A1 (en) * | 1969-03-19 | 1970-10-01 | Basf Ag | herbicide |
| DE1918946A1 (en) * | 1969-04-15 | 1970-10-22 | Basf Ag | herbicide |
-
1972
- 1972-04-13 DE DE2217722A patent/DE2217722C2/en not_active Expired
-
1973
- 1973-03-15 BG BG022999A patent/BG20752A3/en unknown
- 1973-03-15 BG BG024999A patent/BG20277A3/en unknown
- 1973-03-15 BG BG024994A patent/BG20273A3/en unknown
- 1973-03-15 BG BG024997A patent/BG20275A3/en unknown
- 1973-03-15 BG BG024996A patent/BG19364A3/en unknown
- 1973-03-15 BG BG024995A patent/BG20274A3/en unknown
- 1973-03-15 BG BG024998A patent/BG20276A3/en unknown
- 1973-03-15 BG BG025000A patent/BG20278A3/en unknown
- 1973-03-19 JP JP48031078A patent/JPS4914636A/ja active Pending
- 1973-03-20 IL IL41840A patent/IL41840A/en unknown
- 1973-03-21 CA CA166,996A patent/CA1018789A/en not_active Expired
- 1973-03-22 US US343629A patent/US3888655A/en not_active Expired - Lifetime
- 1973-03-23 PH PH14459A patent/PH10948A/en unknown
- 1973-04-03 EG EG123/73A patent/EG11078A/en active
- 1973-04-03 TR TR17279A patent/TR17279A/en unknown
- 1973-04-05 CH CH487773A patent/CH575707A5/xx not_active IP Right Cessation
- 1973-04-06 SE SE7304922A patent/SE388754B/en unknown
- 1973-04-10 NL NLAANVRAGE7304999,A patent/NL182772C/en not_active IP Right Cessation
- 1973-04-11 OA OA54879A patent/OA04402A/en unknown
- 1973-04-11 PL PL1973184054A patent/PL91868B1/en unknown
- 1973-04-11 PL PL1973184050A patent/PL92145B1/en unknown
- 1973-04-11 IT IT49364/73A patent/IT980159B/en active
- 1973-04-11 PL PL1973184055A patent/PL92142B1/en unknown
- 1973-04-11 PL PL1973184051A patent/PL92054B1/en unknown
- 1973-04-11 PL PL1973161846A patent/PL89177B1/en unknown
- 1973-04-11 PL PL1973184053A patent/PL91883B1/en unknown
- 1973-04-11 PL PL1973184052A patent/PL91882B1/en unknown
- 1973-04-11 HU HUBA2909A patent/HU166808B/hu unknown
- 1973-04-12 SU SU2009994A patent/SU522767A3/en active
- 1973-04-12 SU SU2009521A patent/SU535880A3/en active
- 1973-04-12 SU SU2009995A patent/SU500737A3/en active
- 1973-04-12 SU SU2009993A patent/SU495801A3/en active
- 1973-04-12 ES ES413606A patent/ES413606A1/en not_active Expired
- 1973-04-12 SU SU1906703A patent/SU469229A3/en active
- 1973-04-12 GB GB1755373A patent/GB1417279A/en not_active Expired
- 1973-04-12 DK DK199373A patent/DK137702C/en not_active IP Right Cessation
- 1973-04-12 SU SU2009520A patent/SU493056A3/en active
- 1973-04-12 ZA ZA732518A patent/ZA732518B/en unknown
- 1973-04-12 SU SU2009996A patent/SU523626A3/en active
- 1973-04-13 AT AT808174*7A patent/AT327606B/en not_active IP Right Cessation
- 1973-04-13 FR FR7313532A patent/FR2180097B1/fr not_active Expired
- 1973-04-13 CS CS732646A patent/CS192461B2/en unknown
- 1973-04-13 BR BR732710A patent/BR7302710D0/en unknown
- 1973-04-13 BE BE130003A patent/BE798204A/en not_active IP Right Cessation
- 1973-04-13 AT AT808674*7A patent/AT328221B/en not_active IP Right Cessation
- 1973-04-13 AT AT808574*7A patent/AT326947B/en not_active IP Right Cessation
- 1973-04-13 AR AR247543A patent/AR213606A1/en active
- 1973-04-13 AT AT808474A patent/ATA808474A/en unknown
- 1973-04-13 AT AT328573A patent/AT324038B/en not_active IP Right Cessation
- 1973-04-13 AT AT808474*7A patent/AT328220B/en not_active IP Right Cessation
- 1973-04-13 AT AT808174A patent/ATA808174A/en unknown
-
1974
- 1974-03-28 SU SU2009997A patent/SU520012A3/en active
-
1976
- 1976-03-08 SE SE7603082A patent/SE404287B/en not_active IP Right Cessation
- 1976-03-09 SE SE7603124A patent/SE419818B/en not_active IP Right Cessation
- 1976-05-25 KE KE2630*UA patent/KE2630A/en unknown
- 1976-12-30 MY MY183/76A patent/MY7600183A/en unknown
-
1981
- 1981-01-28 JP JP56010282A patent/JPS5915884B2/en not_active Expired
- 1981-01-28 JP JP1028381A patent/JPS56131503A/en active Pending
- 1981-01-28 JP JP1028481A patent/JPS56131504A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6136793U (en) * | 1984-08-10 | 1986-03-07 | 日吉工業株式会社 | Connection structure of high pressure hose and fittings |
| JPS6252390U (en) * | 1985-09-20 | 1987-04-01 | ||
| JPH0464687U (en) * | 1990-10-17 | 1992-06-03 |
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